Canonical Allele Identifier: PA2826594548
Gene: ETFDH HGNC NCBI

Linked Data

ClinVar Variation Id: 529453
ClinVar RCV Id: RCV002528869 RCV000634898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268667.1:p.Ile220Val
CA3122480
NM_001281738.1:c.658A>G